Canonical Allele Identifier: CA2480873232
Gene: IL6R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154448294_154448311delinsGAGTTACCTGTGCTTTTC , CM000663.2:g.154448294_154448311delinsGAGTTACCTGTGCTTTTC GRCh38
NC_000001.10:g.154420770_154420787delinsGAGTTACCTGTGCTTTTC , CM000663.1:g.154420770_154420787delinsGAGTTACCTGTGCTTTTC GRCh37
NC_000001.9:g.152687394_152687411delinsGAGTTACCTGTGCTTTTC NCBI36
NG_012087.1:g.48102_48119delinsGAGTTACCTGTGCTTTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000368485.8:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC MANE Select ENSP00000357470.3:n.996+123_996+140delins...
ENST00000344086.8:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC ENSP00000340589.4:n.996+123_996+140delins...
ENST00000368485.7:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC ENSP00000357470.3:n.996+123_996+140delins...
ENST00000476006.5:c.812+123_812+140delinsGAGTTACCTGTGCTTTTC
ENST00000507256.1:n.194+123_194+140delinsGAGTTACCTGTGCTTTTC
ENST00000515190.1:c.404+123_404+140delinsGAGTTACCTGTGCTTTTC
NM_000565.3:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC NP_000556.1:n.996+123_996+140delinsGAGTTA...
NM_181359.2:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC NP_852004.1:n.996+123_996+140delinsGAGTTA...
XM_005245139.1:c.854+123_854+140delinsGAGTTACCTGTGCTTTTC XP_005245196.1:n.854+123_854+140delinsGAG...
XM_005245140.1:c.854+123_854+140delinsGAGTTACCTGTGCTTTTC XP_005245197.1:n.854+123_854+140delinsGAG...
XM_006711298.1:c.1044+123_1044+140delinsGAGTTACCTGTGCTTTTC XP_006711361.1:n.1044+123_1044+140delinsG...
XM_006711299.2:c.1044+123_1044+140delinsGAGTTACCTGTGCTTTTC XP_006711362.1:n.1044+123_1044+140delinsG...
XM_005245139.2:c.854+123_854+140delinsGAGTTACCTGTGCTTTTC XP_005245196.1:n.854+123_854+140delinsGAG...
XM_005245140.3:c.854+123_854+140delinsGAGTTACCTGTGCTTTTC XP_005245197.1:n.854+123_854+140delinsGAG...
XM_006711298.2:c.1044+123_1044+140delinsGAGTTACCTGTGCTTTTC XP_006711361.1:n.1044+123_1044+140delinsG...
XM_006711299.4:c.1044+123_1044+140delinsGAGTTACCTGTGCTTTTC XP_006711362.1:n.1044+123_1044+140delinsG...
XM_017001199.2:c.1044+123_1044+140delinsGAGTTACCTGTGCTTTTC XP_016856688.1:n.1044+123_1044+140delinsG...
XM_017001200.2:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC XP_016856689.1:n.996+123_996+140delinsGAG...
XM_017001201.2:c.854+123_854+140delinsGAGTTACCTGTGCTTTTC XP_016856690.1:n.854+123_854+140delinsGAG...
NM_000565.4:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC MANE Select NP_000556.1:n.996+123_996+140delinsGAGTTA...
NM_181359.3:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC NP_852004.1:n.996+123_996+140delinsGAGTTA...
NM_001382769.1:c.996+123_996+140delinsGAGTTACCTGTGCTTTTC NP_001369698.1:n.996+123_996+140delinsGAG...
NM_001382770.1:c.1089+123_1089+140delinsGAGTTACCTGTGCTTTTC NP_001369699.1:n.1089+123_1089+140delinsG...
NM_001382771.1:c.1044+123_1044+140delinsGAGTTACCTGTGCTTTTC NP_001369700.1:n.1044+123_1044+140delinsG...
NM_001382772.1:c.990+123_990+140delinsGAGTTACCTGTGCTTTTC NP_001369701.1:n.990+123_990+140delinsGAG...
NM_001382773.1:c.1044+123_1044+140delinsGAGTTACCTGTGCTTTTC NP_001369702.1:n.1044+123_1044+140delinsG...
NM_001382774.1:c.636+123_636+140delinsGAGTTACCTGTGCTTTTC NP_001369703.1:n.636+123_636+140delinsGAG...